Variant report

Variant rs187166503
Chromosome Location chr9:116847063-116847064
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116843000-116858800 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr9:116844800-116851800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr9:116844800-116855400 Weak transcription Gastric stomach
4 chr9:116845000-116847200 Enhancers Fetal Stomach stomach
5 chr9:116845000-116847400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr9:116845200-116849000 Enhancers HepG2 liver
7 chr9:116845200-116850000 Weak transcription Fetal Lung lung
8 chr9:116845200-116854200 Weak transcription Pancreas Pancrea
9 chr9:116845200-116854600 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr9:116845200-116855000 Weak transcription Duodenum Mucosa Duodenum
11 chr9:116845400-116847400 Enhancers A549 lung
12 chr9:116846000-116847200 Enhancers Stomach Smooth Muscle stomach
13 chr9:116846200-116847600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr9:116846200-116848000 Weak transcription Fetal Intestine Small intestine
15 chr9:116846200-116854400 Weak transcription Liver Liver
16 chr9:116846400-116847400 Enhancers Fetal Kidney kidney
17 chr9:116846800-116847600 Enhancers Fetal Muscle Trunk muscle
18 chr9:116847000-116853200 Weak transcription Fetal Intestine Large intestine

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